Mezok Injection (Sodium Benzoate Caffeine)
Caffeine·Sodium Benzoate 110mg
Prescription medication
Myungmoon Pharmaceutical Co., Ltd.
MFDS item code 200403250 · Notified 2004.11.03 · Insurance code 649800701
Relief of headaches as per physician's recommendation, assistive effect on respiratory depression due to alcohol and morphine overdose
First, it is used for headaches caused by spinal nerve stimulation. Second, it is used as an assistive agent to promote respiration when respiratory depression occurs due to alcohol or morphine overdose.
As sodium benzoate caffeine, inject 100 to 500 mg intramuscularly or subcutaneously at a time. In emergencies, intravenous injection may be performed. Adjust according to symptoms.
Since this medication is an injectable solution provided in ampule form, glass fragments may enter the injection solution when cutting the container, which can lead to adverse effects. Particularly, care must be taken to prevent glass fragment contamination when administering to children or the elderly. This medication should be administered with caution to patients with a history of gastric ulcers, heart diseases, glaucoma, and those who show hypersensitivity reactions to this medication. During use, gastrointestinal symptoms such as nausea or diarrhea, cardiovascular symptoms like rapid heartbeat or palpitations, and central nervous system symptoms such as insomnia or anxiety may occur. Additionally, caution is needed for patients with chronic glaucoma, as their symptoms may worsen. In case of overdose, symptoms of depression may worsen in patients with depression, so the dosage should be adjusted to not exceed 1 gram at a time. This medication can interact with other drugs, especially when taken with xanthine drugs, central nervous system stimulants, MAO inhibitors, or cimetidine, which may lead to adverse effects such as central nervous system stimulation or increased blood pressure. Pregnant or nursing women are advised to avoid long-term use of this medication as it can cross the placenta and be excreted in breast milk. For the elderly, as physical functions may be compromised, the dosage should be reduced and used with caution. In case of overdose, severe symptoms such as nausea, vomiting, arrhythmias, convulsions, and respiratory distress may occur, so immediate medical attention is necessary, and if required, professional treatment such as fluid therapy and central nervous system depressants may be needed. When injecting, control the intravenous infusion rate slowly, and use the smallest possible needle. When administering intramuscular or subcutaneous injections, avoid areas where nerves pass, and alternate the injection sites. If severe pain or blood reflux occurs during injection, withdraw the needle immediately and inject at another site.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container at a temperature between 1 degree and 30 degrees Celsius. Proper storage will help maintain the efficacy of the medication and prevent deterioration.
A colorless and transparent ampule containing a colorless liquid
1 ampule (2mL) × 50
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.